Abstract
The large library of organic dye molecules offers almost infinite possibilities for laser design, but still faces a great challenge in achieving pure dye aggregate lasers due to intermolecular quenching. Here, we report a kinetically controlled molecular self-assembly strategy to synthesize unconventional dye microcrystals for lasing. By increasing temperature, the dye self-assembly is transformed from thermodynamic to kinetic control. Unlike the thermodynamic microcrystal products incapable of lasing due to intermolecular charge-transfer-mediated excimer formation, the kinetic dye microcrystals have large intermolecular distances and weak intermolecular interactions, supporting highly efficient intramolecular charge-transfer monomer emission and low-threshold lasing. This work demonstrates single-crystal dye lasers, promising to unleash the full potential of laser dyes in solid-state lasers.
| Original language | English |
|---|---|
| Pages (from-to) | 12345-12351 |
| Number of pages | 7 |
| Journal | ACS Nano |
| Volume | 16 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - 23 Aug 2022 |
| Externally published | Yes |
Keywords
- charge transfer
- intermolecular π-πinteractions
- molecular self-assembly
- organic dye laser
- organic laser
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